Efficacy of ceftolozane in a murine model of Pseudomonas aeruginosa acute pneumonia: in vivo antimicrobial activity and impact on host inflammatory response

J Antimicrob Chemother. 2013 Jan;68(1):177-83. doi: 10.1093/jac/dks343. Epub 2012 Aug 30.

Abstract

Objectives: To assess the activity of ceftolozane, a novel oxyimino-cephalosporin, in comparison with ceftazidime and piperacillin/tazobactam against a multidrug-resistant Pseudomonas aeruginosa strain using a murine model of pneumonia.

Methods: Quantitative bacteriology, survival, histological examination, myeloperoxidase activity, proinflammatory cytokine levels in lungs and endothelial permeability were evaluated to determine the effects of ceftolozane and comparators on P. aeruginosa-induced pneumonia.

Results: After 48 h of treatment, ceftolozane reduced the bacterial load by 3-4 log(10) cfu/g of lung. Systemic dissemination of the pulmonary infection and development of lung damage were inhibited in all β-lactam-treated animals. P. aeruginosa-induced pneumonia led to elevated concentrations of tumour necrosis factor-α, interleukin (IL)-1β and macrophage inflammatory protein (MIP)-2 in the lungs. While the levels of proinflammatory cytokines decreased following ceftazidime and piperacillin/tazobactam therapy, ceftolozane exhibited increased concentrations of IL-1β and MIP-2 after 24 h of infection, resulted in significantly increased levels of recruited neutrophils within the infected lung without increasing lung endothelial permeability.

Conclusions: These data strongly support ceftolozane as an effective option for the treatment of severe P. aeruginosa respiratory infections by improving the early pulmonary inflammatory response without impairing 48 h post-infection homeostasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Animals
  • Anti-Infective Agents / pharmacology*
  • Anti-Infective Agents / therapeutic use
  • Ceftazidime / pharmacology
  • Ceftazidime / therapeutic use
  • Cephalosporins / pharmacology*
  • Cephalosporins / therapeutic use
  • Disease Models, Animal*
  • Drug Resistance, Multiple, Bacterial / drug effects
  • Inflammation / drug therapy
  • Inflammation / microbiology
  • Inflammation / pathology
  • Mice
  • Microbial Sensitivity Tests / methods
  • Pneumonia, Bacterial / drug therapy*
  • Pneumonia, Bacterial / pathology
  • Pseudomonas Infections / drug therapy*
  • Pseudomonas Infections / pathology
  • Pseudomonas aeruginosa / drug effects*
  • Pseudomonas aeruginosa / growth & development
  • Treatment Outcome

Substances

  • Anti-Infective Agents
  • Cephalosporins
  • Ceftazidime